DATA ANALYSIS & RESEARCH MANAGER Salary: £44,000 per annum Reports to: Senior Cancer Intelligence Manager (Prevent and Epidemiology) Department: Policy, Information and Communications Location: Stratford Office, London, w/ high-flex (1 - 2 days per week in the office). We are open to further discussions around flexible working for the successful candidate. Employment type: Permanent Working hours: 35 hours per week. (Compressed Hours or part-time 4 days per week available) Closing date: Sunday 5 May 2024, 23:55 Please note that we may close this role earlier than stated, therefore early application is encouraged to avoid disappointment. At Cancer Research UK, we exist to beat cancer. We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That's why we we're looking for someone talented, someone who shares our vision, someone like you. We are looking for a Data Analysis & Research Manager to join our Cancer Intelligence team. We need you to manage a team of analysts to deliver prevention projects. You'll work with other managers specialising in general epidemiology, early diagnosis, treatment, and cross-cancer pathway work. What will I be doing? Managing projects undertaken by analysts, by liaising with internal teams and other Data Analysis and Research Managers on project need, delivery timelines and outputs Being responsible for general line management and pastoral care of prevention Analysts Managing prevention projects including resource planning and stakeholder management Building strong relationships with other Data Analysis and Research Managers and the Principal Statistician to ensure that projects have the appropriate support Contributing to sign-off on general statistics and press enquiries Developing a project prioritisation approach which meets the needs of Analysts, other Data and Research Managers across Cancer Intelligence, and other internal teams, and communicating decisions about project prioritisation to stakeholders. Managing multiple concurrent projects and being prepared to flex your own and others' workplans to meet business need. What skills are you looking for? Experience of people management and project management Ability to manage own workload and hold self and others accountable for delivery of projects and activity Excellent problem-solving skills Good understanding of best practice analytical techniques Previous experience of delivering analytical projects Proven track record of building and nurturing highly effective relationships Excellent written and verbal communication skills. What will I gain? Each and every one of our employees contributes to our progress and is supporting our work to beat cancer. We think that's impressive. In return, we make sure you are supported by a generous benefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well. Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more. We review pay annually and aim to recognise individual performance and achievements. We don't forget people have lives outside of work too and so we actively encourage a flexible working culture. Our work - from funding cutting-edge research to developing public policy - will change the world. It's exciting to be part of our team. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you quickly, fairly and objectively.
Apr 23, 2024
Full time
DATA ANALYSIS & RESEARCH MANAGER Salary: £44,000 per annum Reports to: Senior Cancer Intelligence Manager (Prevent and Epidemiology) Department: Policy, Information and Communications Location: Stratford Office, London, w/ high-flex (1 - 2 days per week in the office). We are open to further discussions around flexible working for the successful candidate. Employment type: Permanent Working hours: 35 hours per week. (Compressed Hours or part-time 4 days per week available) Closing date: Sunday 5 May 2024, 23:55 Please note that we may close this role earlier than stated, therefore early application is encouraged to avoid disappointment. At Cancer Research UK, we exist to beat cancer. We are professionals with purpose, beating cancer every day. But we need to go much further and much faster. That's why we we're looking for someone talented, someone who shares our vision, someone like you. We are looking for a Data Analysis & Research Manager to join our Cancer Intelligence team. We need you to manage a team of analysts to deliver prevention projects. You'll work with other managers specialising in general epidemiology, early diagnosis, treatment, and cross-cancer pathway work. What will I be doing? Managing projects undertaken by analysts, by liaising with internal teams and other Data Analysis and Research Managers on project need, delivery timelines and outputs Being responsible for general line management and pastoral care of prevention Analysts Managing prevention projects including resource planning and stakeholder management Building strong relationships with other Data Analysis and Research Managers and the Principal Statistician to ensure that projects have the appropriate support Contributing to sign-off on general statistics and press enquiries Developing a project prioritisation approach which meets the needs of Analysts, other Data and Research Managers across Cancer Intelligence, and other internal teams, and communicating decisions about project prioritisation to stakeholders. Managing multiple concurrent projects and being prepared to flex your own and others' workplans to meet business need. What skills are you looking for? Experience of people management and project management Ability to manage own workload and hold self and others accountable for delivery of projects and activity Excellent problem-solving skills Good understanding of best practice analytical techniques Previous experience of delivering analytical projects Proven track record of building and nurturing highly effective relationships Excellent written and verbal communication skills. What will I gain? Each and every one of our employees contributes to our progress and is supporting our work to beat cancer. We think that's impressive. In return, we make sure you are supported by a generous benefits package, a wide range of career and personal development opportunities and high-quality tools, policies and processes to enable you to do your job well. Our benefits package includes a substantial retirement plan, a generous and flexible leave allowance, discounts on anything from travel to technology, gym membership, and much more. We review pay annually and aim to recognise individual performance and achievements. We don't forget people have lives outside of work too and so we actively encourage a flexible working culture. Our work - from funding cutting-edge research to developing public policy - will change the world. It's exciting to be part of our team. How do I apply? We operate an anonymised shortlisting process in our commitment to equality, diversity and inclusion. CVs are required for all applications; but we won't be able to view them until we invite you for an interview. Instead, we ask you to complete the work history section of the online application form for us to be able to assess you quickly, fairly and objectively.
Manager, Biostatistics - FSP team Come discover what our 25,000+ employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work with experts around the world and build the career you've dreamed of. As a part of the Syneos Health team, you'll help us deliver results for a rewarding reason - we improve patients' lives around the world. Because to us, a patient isn't just a number, they're our family, friends, and neighbors. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities • Ensures that the Biostatistics department meets timelines, provides high quality deliverables, complies with contractual project requirements and Standard Operating Procedures (SOPs), and conducts projects within budget. • May participate in the development of department SOPs and guidelines, promoting standardized and consistent processes to maximize the efficiency of the Biostatistical department. • Responsible for staff development, training and retention. Oversees development of direct reports by setting goals, managing performance, evaluating and monitoring training needs, supporting development plans, mentoring, and coaching. • Facilitates succession planning and maintains a Biostatistics staff with diverse skills, abilities, and competencies to meet the business needs of the Biostatistics department. • Makes recommendations for, and participates actively in hiring, onboarding, transferring, and terminating staff. • Maintains a good working knowledge of clinical drug development, ICH, and other regulatory guidelines, and biostatistics in order to effectively serve as a Biostatistics department mentor. Develops and provides training for Biostatistics associates. • Prioritizes activities across Biostatistics projects and facilitates mutually beneficial resolutions to project conflicts between groups or individuals, creating solutions to address business and operational challenges. • Supports the assignment of, or directly assigns Biostatisticians to projects in a manner which keeps associates at their utilization goal and which matches associates to projects appropriate to their skills, training and experience. • May conduct senior review of project deliverables, ensuring that output meets expectations and is consistent with analysis described in study documents. • May be responsible for leading or participating in projects across multiple studies or programs. • May support business development activities. • May participate in, or lead departmental or corporate initiatives. • Performs other work-related duties as assigned. • Minimal travel may be required. What we're looking for • Graduate degree, or equivalent, in biostatistics or related discipline. • Extensive experience in clinical trials or equivalent combination of education and experience with increasing levels of responsibility. • Previous management experience or demonstrated leadership ability preferred. • Extensive knowledge of the drug development process, regulatory requirements and relevant guidelines. • Experience with regulatory submissions preferred. • Ability to read, write, speak, and understand English. • Excellent communication, presentation and interpersonal skills, with an ability to inform, influence, convince, and persuade. Get to know Syneos Health We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health. Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
Sep 23, 2022
Full time
Manager, Biostatistics - FSP team Come discover what our 25,000+ employees already know: work here matters everywhere. We're a growing and evolving biopharmaceutical industry leader, which means you'll have endless opportunities to work with experts around the world and build the career you've dreamed of. As a part of the Syneos Health team, you'll help us deliver results for a rewarding reason - we improve patients' lives around the world. Because to us, a patient isn't just a number, they're our family, friends, and neighbors. Why Syneos Health • means we're committed to our Total Self culture - where everyone can authentically be themselves. Our Total Self culture is what unites us globally, and we know every person's unique contributions make a difference. • We believe our success is a direct result of the people who are driving it - you! We value your dedication to care for our customers and patients, so we want to focus on taking care of you. That's why we offer a comprehensive benefits program encompassing your total health - physical, mental and financial. • We are continuously building the company we all want to work for and our customers want to work with. Why? Because when we bring together diversity of thoughts, backgrounds, cultures, and perspectives - we're able to create a place where everyone feels like they belong. Job responsibilities • Ensures that the Biostatistics department meets timelines, provides high quality deliverables, complies with contractual project requirements and Standard Operating Procedures (SOPs), and conducts projects within budget. • May participate in the development of department SOPs and guidelines, promoting standardized and consistent processes to maximize the efficiency of the Biostatistical department. • Responsible for staff development, training and retention. Oversees development of direct reports by setting goals, managing performance, evaluating and monitoring training needs, supporting development plans, mentoring, and coaching. • Facilitates succession planning and maintains a Biostatistics staff with diverse skills, abilities, and competencies to meet the business needs of the Biostatistics department. • Makes recommendations for, and participates actively in hiring, onboarding, transferring, and terminating staff. • Maintains a good working knowledge of clinical drug development, ICH, and other regulatory guidelines, and biostatistics in order to effectively serve as a Biostatistics department mentor. Develops and provides training for Biostatistics associates. • Prioritizes activities across Biostatistics projects and facilitates mutually beneficial resolutions to project conflicts between groups or individuals, creating solutions to address business and operational challenges. • Supports the assignment of, or directly assigns Biostatisticians to projects in a manner which keeps associates at their utilization goal and which matches associates to projects appropriate to their skills, training and experience. • May conduct senior review of project deliverables, ensuring that output meets expectations and is consistent with analysis described in study documents. • May be responsible for leading or participating in projects across multiple studies or programs. • May support business development activities. • May participate in, or lead departmental or corporate initiatives. • Performs other work-related duties as assigned. • Minimal travel may be required. What we're looking for • Graduate degree, or equivalent, in biostatistics or related discipline. • Extensive experience in clinical trials or equivalent combination of education and experience with increasing levels of responsibility. • Previous management experience or demonstrated leadership ability preferred. • Extensive knowledge of the drug development process, regulatory requirements and relevant guidelines. • Experience with regulatory submissions preferred. • Ability to read, write, speak, and understand English. • Excellent communication, presentation and interpersonal skills, with an ability to inform, influence, convince, and persuade. Get to know Syneos Health We are the only full-service biopharmaceutical solutions company in the world. That means we bring together the best clinical and commercial minds to create a better, smarter, faster way to get medicines into the hands of patients who need it most. Learn more about Syneos Health. Additional Information: Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description. The Company, at its sole discretion, will determine what constitutes as equivalent to the qualifications described above. Further, nothing contained herein should be construed to create an employment contract. Occasionally, required skills/experiences for jobs are expressed in brief terms. Any language contained herein is intended to fully comply with all obligations imposed by the legislation of each country in which it operates, including the implementation of the EU Equality Directive, in relation to the recruitment and employment of its employees. The Company is committed to compliance with the Americans with Disabilities Act, including the provision of reasonable accommodations, when appropriate, to assist employees or applicants to perform the essential functions of the job.
JOB SUMMARY This position is responsible for leading projects across multiple studies or programs. A Senior Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. JOB RESPONSIBILITIES Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR. Prepares Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborate with the sponsor, if required. May be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report. Coordinates the activities of other biostatistics and statistical programming personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. Implements company objectives, and create alternative solutions to address business and operational challenges. Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalate to management. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development and serving as an independent non-voting biostatistician. May lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. Coaches and mentors other Biostatistics staff. Performs other work-related duties as assigned. Minimal travel may be required. QUALIFICATION REQUIREMENTS Graduate degree in biostatistics or related discipline. Moderate experience in clinical trials or an equivalent combination of education and experience. Proficiency in programming. Ability to apply knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research and to effectively communicate statistical concepts. Experience across all statistical tasks required to support clinical trials during the lifecycle of the project, from protocol to CSR. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. "Syneos Health is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Syneos Health is willing to provide reasonable accommodations required for a medical condition or disability."
Sep 23, 2022
Full time
JOB SUMMARY This position is responsible for leading projects across multiple studies or programs. A Senior Biostatistician acts as the primary contact with the sponsor for all biostatistics related activities on assigned projects. JOB RESPONSIBILITIES Provides support across all assigned statistical tasks during the lifecycle of the project, from protocol to CSR. Prepares Statistical Analysis Plans (SAPs), including development of well-presented mock-up displays for tables, listings, and figures. Collaborate with the sponsor, if required. May be responsible for the statistical aspects of the protocol, generation of randomization schedule, publications and input to the clinical study report. Coordinates the activities of other biostatistics and statistical programming personnel on assigned projects to ensure timely completion of high quality work. Provides independent review of project work produced by other biostatisticians in the department. Creates or reviews programming specifications for analysis datasets, tables, listings, and figures. Reviews SAS annotated case report forms (CRFs), database design, and other study documentation to ensure protocol criteria are met and all data is captured as required to support a high quality database and the planned analysis. Conducts and participates in verification and quality control of project deliverables, ensuring that output meets expectations and is consistent with analysis described in SAP and specifications. Implements company objectives, and create alternative solutions to address business and operational challenges. Serves as biostatistics representative on project teams, interfacing as necessary with other departmental project team representatives. This would include preparing in advance for internal meetings, contributing ideas, and demonstrating respect for opinions of others. Manages scheduling and time constraints across multiple projects, sets goals based on priorities from management, adapts to timeline or priority changes by reorganizing daily workload, and proactively communicates to biostatistics management any difficulties with meeting these timelines. Monitors progress on study activities against agreed upon milestones and ensures the study timelines for project deliverables are met. Identifies out of scope tasks and escalate to management. Provides statistical programming support as needed. May participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development and serving as an independent non-voting biostatistician. May lead projects involving integrated analyses, attend regulatory agency meetings or respond to questions, as needed, to support the statistical analysis results of clinical trials on behalf of the sponsor. Follows applicable SOPs, WIs, and relevant regulatory guidelines (e.g. ICH). Maintains well organized, complete, and up-to-date project documentation, and verification/quality control documents and programs; ensuring inspection readiness. Displays willingness to work with others and assists with projects and initiatives as necessary to meet the needs of the business. Supports business development activities by contributing to proposals, budgets, and attending sponsor bid defense meetings. Coaches and mentors other Biostatistics staff. Performs other work-related duties as assigned. Minimal travel may be required. QUALIFICATION REQUIREMENTS Graduate degree in biostatistics or related discipline. Moderate experience in clinical trials or an equivalent combination of education and experience. Proficiency in programming. Ability to apply knowledge of statistical design, analysis, relevant regulatory guidelines, and programming techniques utilized in clinical research and to effectively communicate statistical concepts. Experience across all statistical tasks required to support clinical trials during the lifecycle of the project, from protocol to CSR. Excellent written and verbal communication skills. Ability to read, write, speak, and understand English. "Syneos Health is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. Syneos Health is willing to provide reasonable accommodations required for a medical condition or disability."
Owlstone Medical ( ()) is on a mission to save 100,000 lives and $1.5 billion in healthcare costs through the development and application of Breath Biopsy , which enables the non-invasive collection and analysis of biomarkers in exhaled breath for early disease detection and precision medicine. We are currently seeking a Senior Biostatistician with clinical research and biomarker discovery experience to be a member of our Clinical and Translational Science Department. The candidate will contribute to the mission of the company by providing input into clinical study designs and trial protocols and will ensure that data analysis and interpretation of results are statistically sound and meet the desired study objectives. The Senior Biostatistician will work in a cross-functional team to support Owlstone s clinical test development and customer services business. Key responsibilities: Perform appropriate statistical analyses at all phases of the project, from clinical protocol development and study design through final analysis and reporting of results Evaluate clinical research studies and prepare statistical analysis plans that provide sound approaches to support a continuum of study goals, from biomarker discovery through clinical test development Apply appropriate statistical methodologies to analyze the data, including, but not limited to, hypothesis testing, regression models, multivariate analyses, machine learning, and network-based analyses Program and analyze data using Python or R; demonstrate good programming practices through proper documentation and commenting; perform appropriate QA to ensure accuracy and consistency of results Effectively communicate statistical methods and results to cross-functional team members, clinical collaborators, and others with a variety of technical expertise (including lay audience) Maintaining technical knowledge and skills appropriate for the role, including staying current with innovative statistical methodologies that are relevant to clinical research Requirements Technical Competencies: A thorough understanding of sample size, study power, precision, and their application in clinical trials and/or observational studies Proficient in translating clinical research questions into testable hypotheses Adept in communicating the assumptions, limitations, and advantages or disadvantages of statistical methods and describing preferred alternatives when key assumptions are not met Working proficiency in Python (to the level of package writing) or R (capable of implementing statistical or computational methods) Demonstrated ability to take initiative and be proactive in your approach to work, with an independent, creative, and open mindset Desirable Experience: Statistical experience working with CROs or the biopharmaceutical industry Application of statistical design and analysis for biomarker discovery and validation Experience with metabolomics (or other omics) data from clinical or epidemiologic studies Experience working closely with clinical biologists and translational scientists to analyze and interpret clinical datasets Strong publication record or other demonstrable track record of performance and collaboration Familiarity with IRB/ethics and regulatory documentation Qualifications: PhD or equivalent combination of education, training and experience in (bio) statistics or a related discipline, preferably with demonstrable experience working in a clinical, biomedical, or commercial environment
Sep 22, 2022
Full time
Owlstone Medical ( ()) is on a mission to save 100,000 lives and $1.5 billion in healthcare costs through the development and application of Breath Biopsy , which enables the non-invasive collection and analysis of biomarkers in exhaled breath for early disease detection and precision medicine. We are currently seeking a Senior Biostatistician with clinical research and biomarker discovery experience to be a member of our Clinical and Translational Science Department. The candidate will contribute to the mission of the company by providing input into clinical study designs and trial protocols and will ensure that data analysis and interpretation of results are statistically sound and meet the desired study objectives. The Senior Biostatistician will work in a cross-functional team to support Owlstone s clinical test development and customer services business. Key responsibilities: Perform appropriate statistical analyses at all phases of the project, from clinical protocol development and study design through final analysis and reporting of results Evaluate clinical research studies and prepare statistical analysis plans that provide sound approaches to support a continuum of study goals, from biomarker discovery through clinical test development Apply appropriate statistical methodologies to analyze the data, including, but not limited to, hypothesis testing, regression models, multivariate analyses, machine learning, and network-based analyses Program and analyze data using Python or R; demonstrate good programming practices through proper documentation and commenting; perform appropriate QA to ensure accuracy and consistency of results Effectively communicate statistical methods and results to cross-functional team members, clinical collaborators, and others with a variety of technical expertise (including lay audience) Maintaining technical knowledge and skills appropriate for the role, including staying current with innovative statistical methodologies that are relevant to clinical research Requirements Technical Competencies: A thorough understanding of sample size, study power, precision, and their application in clinical trials and/or observational studies Proficient in translating clinical research questions into testable hypotheses Adept in communicating the assumptions, limitations, and advantages or disadvantages of statistical methods and describing preferred alternatives when key assumptions are not met Working proficiency in Python (to the level of package writing) or R (capable of implementing statistical or computational methods) Demonstrated ability to take initiative and be proactive in your approach to work, with an independent, creative, and open mindset Desirable Experience: Statistical experience working with CROs or the biopharmaceutical industry Application of statistical design and analysis for biomarker discovery and validation Experience with metabolomics (or other omics) data from clinical or epidemiologic studies Experience working closely with clinical biologists and translational scientists to analyze and interpret clinical datasets Strong publication record or other demonstrable track record of performance and collaboration Familiarity with IRB/ethics and regulatory documentation Qualifications: PhD or equivalent combination of education, training and experience in (bio) statistics or a related discipline, preferably with demonstrable experience working in a clinical, biomedical, or commercial environment
The Health Foundation is an independent charity committed to bringing about better health and health care for people in the UK. The Data Architect will work in the Improvement Analytics Unit (IAU) which is part of the Data Analytics team. The team conducts high-quality, in-house research and analysis, and collaborates with the NHS to develop approaches to improve health care that can be applied at local and national levels. Specifically, the successful candidate will support the IAU, a joint unit with NHS England that provides rapid feedback about the effects of new models of care and develops robust approaches to data management and information governance, applying analytics directly to real-world problems. The successful applicant will work together with the Senior Data Manager to develop and deliver an ambitious data management agenda to support rapid-cycle evaluation. The Data Architect will help ensure that quality control, standardised cleaning and metadata collection is applied to the updating of core datasets used by the IAU, as well as help investigate the potential and use of new data. The Data Architect will also work closely with statisticians and analysts in the team during the research and development phase of individual evaluations to develop and deliver data specifications and analysis datasets used by the IAU. They will also help to embed the preferred approach to analysis within the production environment. Since the IAU has a complex and dynamic work programme, it is essential to be adaptive and to seek to improve approaches to data management over time. At all times the post holder will aim to embed our key behaviours - working together, achieving impact, discovering and learning - in all aspects of their day-to-day delivery in the role. The Data Architect will be part of a growing group of data management professionals who support work across the Data Analytics directorate, collaborating with a wide range of internal and external partners. To find out more about the role and what we are looking for, please click on the apply link below to be redirected to our careers website.
Sep 19, 2022
Full time
The Health Foundation is an independent charity committed to bringing about better health and health care for people in the UK. The Data Architect will work in the Improvement Analytics Unit (IAU) which is part of the Data Analytics team. The team conducts high-quality, in-house research and analysis, and collaborates with the NHS to develop approaches to improve health care that can be applied at local and national levels. Specifically, the successful candidate will support the IAU, a joint unit with NHS England that provides rapid feedback about the effects of new models of care and develops robust approaches to data management and information governance, applying analytics directly to real-world problems. The successful applicant will work together with the Senior Data Manager to develop and deliver an ambitious data management agenda to support rapid-cycle evaluation. The Data Architect will help ensure that quality control, standardised cleaning and metadata collection is applied to the updating of core datasets used by the IAU, as well as help investigate the potential and use of new data. The Data Architect will also work closely with statisticians and analysts in the team during the research and development phase of individual evaluations to develop and deliver data specifications and analysis datasets used by the IAU. They will also help to embed the preferred approach to analysis within the production environment. Since the IAU has a complex and dynamic work programme, it is essential to be adaptive and to seek to improve approaches to data management over time. At all times the post holder will aim to embed our key behaviours - working together, achieving impact, discovering and learning - in all aspects of their day-to-day delivery in the role. The Data Architect will be part of a growing group of data management professionals who support work across the Data Analytics directorate, collaborating with a wide range of internal and external partners. To find out more about the role and what we are looking for, please click on the apply link below to be redirected to our careers website.
As a leader in next generation, data-driven pharmaceutical services, Cytel is shaping the future of clinical development. We deliver to the market high impact statistical consultancy on clinical development plans and individual trials, innovative analytical software for statistical analysis and simulation, and best-in-class data science analytics services. Our culture is inclusive, collaborative and results-driven with a shared commitment to quality. With operations across North America, Europe, and Asia, Cytel hires passionate and talented people who share its mission of ensuring the development of safe and effective health technologies. We are hiring a Managing Consultant to join our Strategic Consulting Practice. As a seasoned Biostatistician, you will leverage and broaden Cytel's reputation for thought leadership and innovative services by leading engagements for pharmaceutical, biotech and device clients, and building and maintaining successful long-term relationships with clients in collaboration with Cytel's business developers and other personnel related to the account. This includes developing and demonstrating thought leadership in statistical methodology for clinical development, ensuring that Cytel remains at the leading edge, and raising Cytel brand awareness and recognition throughout the industry. Specifically, we are looking for leaders with a strong foundation in statistics plus broad expertise and/or unique knowledge in related areas (adaptive designs, clinical development, data science, model-informed drug development), to provide strategic advice to define optimal regulatory, clinical and/or market access pathways and promote faster patient access to better health technologies. * Specific duties and responsibilities: * * Provides strategic advice on client projects, collaborating with an integrated team of Strategic Consultants and Analysts to define optimal regulatory, clinical and/or market access pathways. Adapts precedent and develops innovative solutions impartially selecting and combining traditional and novel approaches. * Assumes overall responsibility for assigned Strategic Consulting accounts and projects, acting as the client's primary point of contact for Strategic Consulting engagements, developing mutually beneficial partnerships and taking ownership for the strategic needs of the client. * Depending on experience, creates, identifies and pursues new business opportunities both within Strategic Consulting and across Cytel Business Units by identifying emerging customer needs and formulating appropriate solutions to meet revenue, profitability and customer satisfaction objectives. * The position requires regular travel, substantial direct contact with senior management and executives at prospects and existing clients, and the ability to build and leverage strong interpersonal business relationships both internally and externally to Cytel. * Qualifications and Experience: * * Thorough understanding of the biopharmaceutical R&D process in combination with solid business acumen and an appreciation of the broader business issues. * Strategic thinker with a global orientation, strong problem-solving and analytical skills, and the ability to execute in complex situations at the tactical level. * Comfortable presenting and interfacing with senior executives within the clients. * Experience interacting with regulatory agencies (FDA/EMA) and key opinion leaders to enhance development plans. * Proven management skills with the ability to build, mentor and motivate a strong team of consultants and analysts. * Collaborative, entrepreneurial and self-motivated, with an understanding of the dynamics of high-growth companies; the ability to work effectively in a challenging and sometimes rapidly changing environment. * Minimum of a Masters (PhD desirable) in Mathematics, Biostatistics or a related field; MBA, MD or advanced degree highly desirable; at least 10-15 years of experience in the clinical trials or health research environment. * Why Cytel? * * You will have the opportunity to play an integral role helping our clients and the industry shape the future of drug development * You will be part of an exciting new chapter in Cytel's history with high growth and opportunities to progress to leadership positions within the company * You will work with and leverage the best and brightest minds in the industry . #LI-KO1
Feb 26, 2022
Full time
As a leader in next generation, data-driven pharmaceutical services, Cytel is shaping the future of clinical development. We deliver to the market high impact statistical consultancy on clinical development plans and individual trials, innovative analytical software for statistical analysis and simulation, and best-in-class data science analytics services. Our culture is inclusive, collaborative and results-driven with a shared commitment to quality. With operations across North America, Europe, and Asia, Cytel hires passionate and talented people who share its mission of ensuring the development of safe and effective health technologies. We are hiring a Managing Consultant to join our Strategic Consulting Practice. As a seasoned Biostatistician, you will leverage and broaden Cytel's reputation for thought leadership and innovative services by leading engagements for pharmaceutical, biotech and device clients, and building and maintaining successful long-term relationships with clients in collaboration with Cytel's business developers and other personnel related to the account. This includes developing and demonstrating thought leadership in statistical methodology for clinical development, ensuring that Cytel remains at the leading edge, and raising Cytel brand awareness and recognition throughout the industry. Specifically, we are looking for leaders with a strong foundation in statistics plus broad expertise and/or unique knowledge in related areas (adaptive designs, clinical development, data science, model-informed drug development), to provide strategic advice to define optimal regulatory, clinical and/or market access pathways and promote faster patient access to better health technologies. * Specific duties and responsibilities: * * Provides strategic advice on client projects, collaborating with an integrated team of Strategic Consultants and Analysts to define optimal regulatory, clinical and/or market access pathways. Adapts precedent and develops innovative solutions impartially selecting and combining traditional and novel approaches. * Assumes overall responsibility for assigned Strategic Consulting accounts and projects, acting as the client's primary point of contact for Strategic Consulting engagements, developing mutually beneficial partnerships and taking ownership for the strategic needs of the client. * Depending on experience, creates, identifies and pursues new business opportunities both within Strategic Consulting and across Cytel Business Units by identifying emerging customer needs and formulating appropriate solutions to meet revenue, profitability and customer satisfaction objectives. * The position requires regular travel, substantial direct contact with senior management and executives at prospects and existing clients, and the ability to build and leverage strong interpersonal business relationships both internally and externally to Cytel. * Qualifications and Experience: * * Thorough understanding of the biopharmaceutical R&D process in combination with solid business acumen and an appreciation of the broader business issues. * Strategic thinker with a global orientation, strong problem-solving and analytical skills, and the ability to execute in complex situations at the tactical level. * Comfortable presenting and interfacing with senior executives within the clients. * Experience interacting with regulatory agencies (FDA/EMA) and key opinion leaders to enhance development plans. * Proven management skills with the ability to build, mentor and motivate a strong team of consultants and analysts. * Collaborative, entrepreneurial and self-motivated, with an understanding of the dynamics of high-growth companies; the ability to work effectively in a challenging and sometimes rapidly changing environment. * Minimum of a Masters (PhD desirable) in Mathematics, Biostatistics or a related field; MBA, MD or advanced degree highly desirable; at least 10-15 years of experience in the clinical trials or health research environment. * Why Cytel? * * You will have the opportunity to play an integral role helping our clients and the industry shape the future of drug development * You will be part of an exciting new chapter in Cytel's history with high growth and opportunities to progress to leadership positions within the company * You will work with and leverage the best and brightest minds in the industry . #LI-KO1
CK Group is recruiting for a Senior Biostatistician to join a specialist CRO. Working from home is available. Senior Biostatistician Role: Develop SAS programs to create derived variables and analysis data sets and computer programs to generate listings, tables, and graphs using SAS Independently utilize your respected expertise to provide statistical consulting Prepare statistical sections of protoc...... click apply for full job details
Jan 04, 2022
Full time
CK Group is recruiting for a Senior Biostatistician to join a specialist CRO. Working from home is available. Senior Biostatistician Role: Develop SAS programs to create derived variables and analysis data sets and computer programs to generate listings, tables, and graphs using SAS Independently utilize your respected expertise to provide statistical consulting Prepare statistical sections of protoc...... click apply for full job details
Want to do the best work of your life? With 24 million customers in 6 countries, make your mark at Europe's leading media and entertainment brand. A workplace where you can proudly be yourself; our people make Sky a truly exciting and inclusive place to work. What you'll do: * Development of hardware/software systems, primarily in a software development role * Providing Technical Lead on some Projects, working closely with the Solutions Architect and Development Managers. * Ability to work in both the front and back end, across the full stack. * Ability to craft both front end apps and service oriented back ends. This will be done in conjunction with the Solutions Architect. * Liaison with designers, statisticians, technical directors, studio production staff, programme makers, and a wide cross-section of the business * Collaborate closely with Stakeholders and Support to ensure that effective and up-to-date documentation is available for all systems * Proactively monitoring systems to ensure accurate operation What you'll bring: * 2.1 bachelor's degree or higher in a technical subject, or ability to demonstrate similar levels of knowledge through on-the-job experience. * Experience of multiple object-orientated programming languages including both C# and JavaScript; understanding of how to write and modularise JavaScript is essential * Very strong understanding of the .Net framework, HTML5, relational database systems (SQL or Oracle) * Strong understanding of version control tools like TFS and other development tools, * Experience of Single Page Web Apps, Web Services, Windows Services Team Overview Group Product is the team behind the world-class Sky products line-up. From Sky+ to Sky Q. From hardware and software to intricate design, we're proud that everyone's favourite Sky products are #MadeByUs The Rewards: There's a reason people can't stop talking about #LifeAtSky. Our phenomenal range of rewards really are something special, here are just a few: * Sky Q, for the TV you love all in one place * A generous pension package * Private healthcare * Discounted mobile and broadband * Access a wide range of exclusive Sky VIP rewards and experiences Where you'll work: Osterley: Our Osterley Campus is a 10-minute walk from Syon Lane train station. Or you can hop on one of our free shuttle buses that run to and from Osterley, Gunnersbury, Ealing Broadway and South Ealing tube stations. There's also plenty of bike shelters and showers. On campus, you'll find 13 subsidised restaurants, cafes, and a Waitrose. You can keep in shape at our subsidised gym, catch the latest shows and movies at our cinema, get your car washed and even get pampered at our beauty salon. Inclusion: We take pride in our approach to diversity and inclusion: we've been recognised by The Times and Stonewall for this, and we've committed £30million to support the fight against racial injustice. We've also set ambitious targets for increasing ethnic diversity and representation throughout our organisation. At Sky we don't just look at your CV. We're more focused on who you are and your potential. We also know that everyone has a life outside work, so we're happy to discuss flexible working. And we'll do everything we can to support you during your application. If you need us to make any adjustments to our recruitment process, speak to our recruitment team who will be happy to support you. Why wait? Apply now to build an amazing career and be part of a brilliant team. We can't wait to hear from you. To find out more about working with us, search #LifeAtSky on social media. A job you love to talk about. Just so you know: if your application is successful, we'll ask you to complete a criminal record check. And depending on the role you have applied for and the nature of any convictions you may have, we might have to withdraw the offer.
Dec 08, 2021
Full time
Want to do the best work of your life? With 24 million customers in 6 countries, make your mark at Europe's leading media and entertainment brand. A workplace where you can proudly be yourself; our people make Sky a truly exciting and inclusive place to work. What you'll do: * Development of hardware/software systems, primarily in a software development role * Providing Technical Lead on some Projects, working closely with the Solutions Architect and Development Managers. * Ability to work in both the front and back end, across the full stack. * Ability to craft both front end apps and service oriented back ends. This will be done in conjunction with the Solutions Architect. * Liaison with designers, statisticians, technical directors, studio production staff, programme makers, and a wide cross-section of the business * Collaborate closely with Stakeholders and Support to ensure that effective and up-to-date documentation is available for all systems * Proactively monitoring systems to ensure accurate operation What you'll bring: * 2.1 bachelor's degree or higher in a technical subject, or ability to demonstrate similar levels of knowledge through on-the-job experience. * Experience of multiple object-orientated programming languages including both C# and JavaScript; understanding of how to write and modularise JavaScript is essential * Very strong understanding of the .Net framework, HTML5, relational database systems (SQL or Oracle) * Strong understanding of version control tools like TFS and other development tools, * Experience of Single Page Web Apps, Web Services, Windows Services Team Overview Group Product is the team behind the world-class Sky products line-up. From Sky+ to Sky Q. From hardware and software to intricate design, we're proud that everyone's favourite Sky products are #MadeByUs The Rewards: There's a reason people can't stop talking about #LifeAtSky. Our phenomenal range of rewards really are something special, here are just a few: * Sky Q, for the TV you love all in one place * A generous pension package * Private healthcare * Discounted mobile and broadband * Access a wide range of exclusive Sky VIP rewards and experiences Where you'll work: Osterley: Our Osterley Campus is a 10-minute walk from Syon Lane train station. Or you can hop on one of our free shuttle buses that run to and from Osterley, Gunnersbury, Ealing Broadway and South Ealing tube stations. There's also plenty of bike shelters and showers. On campus, you'll find 13 subsidised restaurants, cafes, and a Waitrose. You can keep in shape at our subsidised gym, catch the latest shows and movies at our cinema, get your car washed and even get pampered at our beauty salon. Inclusion: We take pride in our approach to diversity and inclusion: we've been recognised by The Times and Stonewall for this, and we've committed £30million to support the fight against racial injustice. We've also set ambitious targets for increasing ethnic diversity and representation throughout our organisation. At Sky we don't just look at your CV. We're more focused on who you are and your potential. We also know that everyone has a life outside work, so we're happy to discuss flexible working. And we'll do everything we can to support you during your application. If you need us to make any adjustments to our recruitment process, speak to our recruitment team who will be happy to support you. Why wait? Apply now to build an amazing career and be part of a brilliant team. We can't wait to hear from you. To find out more about working with us, search #LifeAtSky on social media. A job you love to talk about. Just so you know: if your application is successful, we'll ask you to complete a criminal record check. And depending on the role you have applied for and the nature of any convictions you may have, we might have to withdraw the offer.
About Us Our clients come to us for best in class forecasting and analysis of economic conditions and an understanding of risks to business success in the regions where they operate. Our global team of analysts, economists and subject matter experts provide economy-wide insight on the drivers of economic growth and industry performance. Our consulting team of economists are highly regarded for their ability to translate economic events into direct drivers of business activity and economic impact. We are looking for a dynamic, business development professional to drive new business and scale development of solution design for our Economics and Country Risk (ECR) offerings to corporate, financial and government clients. Candidate will be responsible for developing new and enhanced analytical approaches within the following portfolios: Business Analytics and Forecasting Market Sizing & Segmentation Market Entry Analysis Economic/Fiscal/Policy Analysis Labour Markets/Workforce Analysis Trade Policy & Analysis Macroeconomic Modelling & Scenario Planning Economic Development Strategy Your Role As part of the Economics & Country Risk Consulting team, the successful candidate will have commercial responsibility for collaborating with the team of economists, statisticians and subject matter experts in pursuit of new data-driven client solutions. You will be expected to provide solutions across diverse industry sectors with a focus on supporting demand planning within client workflows. Success in this role involves partnering with internal resources such as Sales, Research teams, external project partners and Sales Operations to support technical and business development initiatives. We're looking for an experienced commercial professional who: Is comfortable discussing analytical techniques to reveal new insight and uncover new value to customers Feels comfortable interacting with senior executives Can learn and effectively position a wide range of ECR persona/workflow solutions and articulate IHS Markit's value proposition Is capable of architecting a client solution 1) based on client pain-points; 2) integrating recommendations from the Applied Economics consulting teams; and 3) replicating these solutions at scale across a swath of clients with similar requirements Enjoys networking at industry events and can quickly develop new business relationships Can contribute to go-to-market strategies with suggestions for marketing campaigns, events, account planning, customer segmentation and structured sales activities About You Key Qualifications and Skills: Intellectual curiosity with agility to solve business challenges across a range of client types Minimum 10 years of business to business sales experience Strong written and verbal communication skills, with the ability to tailor communications to audience needs Proven excellent interpersonal skills with an ability to build effective internal and external relationships Experience selling business and information services (research, data, consulting) Willingness to travel internationally up to 25% during normal times necessary to conduct face-to-face meetings or attend industry conferences Bachelor's degree minimum, advanced degree preferred What we offer Cash incentive plan Options to work from home Flexible working hours to allow you to attend your family Opportunity to work with world experts in the field Strong client base and broad product line Inclusion and diversity are critical to the success of IHS Markit, and we actively encourage applications from people of all backgrounds. We are committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, status as a protected veteran, or any other protected category. For more information on the many ways in which we enthusiastically support inclusion and diversity efforts for both candidates and employees, please access our Inclusion & Diversity Statement here . We are proud to provide reasonable accommodations to applicants with disabilities. If you are interested in applying for employment with IHS Markit and need special assistance or an accommodation to use our website or to apply for a position, please contact or call +1 . Determination on requests for reasonable accommodation are considered on a case-by-case basis. This contact information (email and phone) is intended for application assistance and accommodation requests only. We are unable to accept resumes or provide information about application status through the phone number or email address above. Resumes are only accepted through the online application process, and only qualified candidates will receive consideration and follow-up. IHS Markit maintains a substance-free workplace; employees may be asked to submit to a drug test (where permitted by law). In addition, as a federal contractor in the United States, the company participates in the E-Verify Program to confirm eligibility to work. For information please click on the following links: IHS Markit Business Code of Conduct Right to Work EEO is the Law EEO is the Law Supplement Pay Transparency Current Colleagues If you are currently employed by IHS Markit, please apply internally via the Workday internal careers site.
Dec 07, 2021
Full time
About Us Our clients come to us for best in class forecasting and analysis of economic conditions and an understanding of risks to business success in the regions where they operate. Our global team of analysts, economists and subject matter experts provide economy-wide insight on the drivers of economic growth and industry performance. Our consulting team of economists are highly regarded for their ability to translate economic events into direct drivers of business activity and economic impact. We are looking for a dynamic, business development professional to drive new business and scale development of solution design for our Economics and Country Risk (ECR) offerings to corporate, financial and government clients. Candidate will be responsible for developing new and enhanced analytical approaches within the following portfolios: Business Analytics and Forecasting Market Sizing & Segmentation Market Entry Analysis Economic/Fiscal/Policy Analysis Labour Markets/Workforce Analysis Trade Policy & Analysis Macroeconomic Modelling & Scenario Planning Economic Development Strategy Your Role As part of the Economics & Country Risk Consulting team, the successful candidate will have commercial responsibility for collaborating with the team of economists, statisticians and subject matter experts in pursuit of new data-driven client solutions. You will be expected to provide solutions across diverse industry sectors with a focus on supporting demand planning within client workflows. Success in this role involves partnering with internal resources such as Sales, Research teams, external project partners and Sales Operations to support technical and business development initiatives. We're looking for an experienced commercial professional who: Is comfortable discussing analytical techniques to reveal new insight and uncover new value to customers Feels comfortable interacting with senior executives Can learn and effectively position a wide range of ECR persona/workflow solutions and articulate IHS Markit's value proposition Is capable of architecting a client solution 1) based on client pain-points; 2) integrating recommendations from the Applied Economics consulting teams; and 3) replicating these solutions at scale across a swath of clients with similar requirements Enjoys networking at industry events and can quickly develop new business relationships Can contribute to go-to-market strategies with suggestions for marketing campaigns, events, account planning, customer segmentation and structured sales activities About You Key Qualifications and Skills: Intellectual curiosity with agility to solve business challenges across a range of client types Minimum 10 years of business to business sales experience Strong written and verbal communication skills, with the ability to tailor communications to audience needs Proven excellent interpersonal skills with an ability to build effective internal and external relationships Experience selling business and information services (research, data, consulting) Willingness to travel internationally up to 25% during normal times necessary to conduct face-to-face meetings or attend industry conferences Bachelor's degree minimum, advanced degree preferred What we offer Cash incentive plan Options to work from home Flexible working hours to allow you to attend your family Opportunity to work with world experts in the field Strong client base and broad product line Inclusion and diversity are critical to the success of IHS Markit, and we actively encourage applications from people of all backgrounds. We are committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, status as a protected veteran, or any other protected category. For more information on the many ways in which we enthusiastically support inclusion and diversity efforts for both candidates and employees, please access our Inclusion & Diversity Statement here . We are proud to provide reasonable accommodations to applicants with disabilities. If you are interested in applying for employment with IHS Markit and need special assistance or an accommodation to use our website or to apply for a position, please contact or call +1 . Determination on requests for reasonable accommodation are considered on a case-by-case basis. This contact information (email and phone) is intended for application assistance and accommodation requests only. We are unable to accept resumes or provide information about application status through the phone number or email address above. Resumes are only accepted through the online application process, and only qualified candidates will receive consideration and follow-up. IHS Markit maintains a substance-free workplace; employees may be asked to submit to a drug test (where permitted by law). In addition, as a federal contractor in the United States, the company participates in the E-Verify Program to confirm eligibility to work. For information please click on the following links: IHS Markit Business Code of Conduct Right to Work EEO is the Law EEO is the Law Supplement Pay Transparency Current Colleagues If you are currently employed by IHS Markit, please apply internally via the Workday internal careers site.
Geoff King at RBW Consulting is recruiting for a Senior or Principal Statistician to join a market leading immunology business with specialist experience in the research and development of allergy treatments as they look to continue on an exciting period of growth for the company. This mid-size organisation are passionate in their ambition to transform patients' lives through the ideas and products they bring to market covering such life impacting areas such as hayfever, pet and food allergies. With an exciting and varied pipeline from Phase I - III and post marketing this is a great time to join an organisation which is sure to become a household name. As sole Statistician you will play an important part in delivering these important and life changing drugs to market. In addition to working on being the lead Statistician on multiple projects you will review / author SAPs, sections of the clinical study report and act as primary point of contact with all CRO/vendors for all biostatistics related activities. If you are an experienced and driven Biostatistician who wants to have a direct impact on the successful launch of life changing treatments and are able to work flexibly across a multi-functional and collaborative team then this would be a fantastic opportunity for you. *Main duties & responsibilities:* * Lead statistician for multiple projects. * Responsible for all statistical aspects of clinical trial including trial design, programming, analysis and regulatory filing strategy. * Collaborates with applicable study team members in the process of outlining the clinical development. * Authors and/or reviews Statistical Analysis Plans (SAPs). * Authors/reviews sections of the clinical study report. * Acts as the primary contact with CRO/Vendors for all biostatistics related activities on assigned projects. *Key requirements:* * PhD or MSc in Statistics or Biostatistics combined with relevant experience within the pharmaceutical industry. * Advanced knowledge of clinical study designs and common statistical analysis methods. * Extensive knowledge of MHRA, FDA and ICH regulations and industry standards. * Good knowledge of statistical programming languages and statistical software (eg. SAS, R, East etc). * Excellent communication skills. * Positive "can do" attitude. A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page.
Mar 23, 2021
Full time
Geoff King at RBW Consulting is recruiting for a Senior or Principal Statistician to join a market leading immunology business with specialist experience in the research and development of allergy treatments as they look to continue on an exciting period of growth for the company. This mid-size organisation are passionate in their ambition to transform patients' lives through the ideas and products they bring to market covering such life impacting areas such as hayfever, pet and food allergies. With an exciting and varied pipeline from Phase I - III and post marketing this is a great time to join an organisation which is sure to become a household name. As sole Statistician you will play an important part in delivering these important and life changing drugs to market. In addition to working on being the lead Statistician on multiple projects you will review / author SAPs, sections of the clinical study report and act as primary point of contact with all CRO/vendors for all biostatistics related activities. If you are an experienced and driven Biostatistician who wants to have a direct impact on the successful launch of life changing treatments and are able to work flexibly across a multi-functional and collaborative team then this would be a fantastic opportunity for you. *Main duties & responsibilities:* * Lead statistician for multiple projects. * Responsible for all statistical aspects of clinical trial including trial design, programming, analysis and regulatory filing strategy. * Collaborates with applicable study team members in the process of outlining the clinical development. * Authors and/or reviews Statistical Analysis Plans (SAPs). * Authors/reviews sections of the clinical study report. * Acts as the primary contact with CRO/Vendors for all biostatistics related activities on assigned projects. *Key requirements:* * PhD or MSc in Statistics or Biostatistics combined with relevant experience within the pharmaceutical industry. * Advanced knowledge of clinical study designs and common statistical analysis methods. * Extensive knowledge of MHRA, FDA and ICH regulations and industry standards. * Good knowledge of statistical programming languages and statistical software (eg. SAS, R, East etc). * Excellent communication skills. * Positive "can do" attitude. A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page.
Geoff King at RBW Consulting is working with a specialist Clinical Research Organisation to the pharmaceutical industry in the recruitment of multiple Senior or Principal Biostatisticians to join their FSP and embedded model teams as they continue to support a number of the worlds most cutting edge pharmaceutical companies. As a CRO focused on delivering high quality statistics and programming support to these companies you will have the opportunity to work across multiple therapeutic area on phase I-IV clinical trials. This company prides themselves on their friendly and supportive culture where you will receive help on trials no matter how big or small the request. They also provide constant opportunities for promotion and growth due to their investment on staff and defined career plans. *Main duties & responsibilities:* • Perform technical and consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs. • Author simple and complex study SAP and TFL shells. • Author and review simple and complex dataset standards. • Perform data checks and data exploration (e.g. using frequencies, histograms). • Identify data and standards issues and resolve or escalate as appropriate. • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice. • Application of complex statistical techniques (e.g. mixed effects, non-linear modelling, Bayesian, advanced survival), model checking and interpretation. • Perform literature review and ability to extract and collate relevant information and data from external papers as needed. • Identify and implement appropriate sample size method using software or simulations. • Support study team in providing study design options. • Review of project management related documents. • Maintain study master file documents and any other documents that are required to be audit ready. • Lead internal and client study team meetings effectively. *Key requirements:* • MSc or PhD in Statistics/Biostatistics (or equivalent). • At least 3 years of relevant industry experience. • Understanding of clinical drug development process, relevant disease areas, endpoints and different study designs. • Awareness of industry and project standards & ICH guidelines. • Excellent verbal and written communication skills. A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page.
Mar 23, 2021
Full time
Geoff King at RBW Consulting is working with a specialist Clinical Research Organisation to the pharmaceutical industry in the recruitment of multiple Senior or Principal Biostatisticians to join their FSP and embedded model teams as they continue to support a number of the worlds most cutting edge pharmaceutical companies. As a CRO focused on delivering high quality statistics and programming support to these companies you will have the opportunity to work across multiple therapeutic area on phase I-IV clinical trials. This company prides themselves on their friendly and supportive culture where you will receive help on trials no matter how big or small the request. They also provide constant opportunities for promotion and growth due to their investment on staff and defined career plans. *Main duties & responsibilities:* • Perform technical and consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs. • Author simple and complex study SAP and TFL shells. • Author and review simple and complex dataset standards. • Perform data checks and data exploration (e.g. using frequencies, histograms). • Identify data and standards issues and resolve or escalate as appropriate. • Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice. • Application of complex statistical techniques (e.g. mixed effects, non-linear modelling, Bayesian, advanced survival), model checking and interpretation. • Perform literature review and ability to extract and collate relevant information and data from external papers as needed. • Identify and implement appropriate sample size method using software or simulations. • Support study team in providing study design options. • Review of project management related documents. • Maintain study master file documents and any other documents that are required to be audit ready. • Lead internal and client study team meetings effectively. *Key requirements:* • MSc or PhD in Statistics/Biostatistics (or equivalent). • At least 3 years of relevant industry experience. • Understanding of clinical drug development process, relevant disease areas, endpoints and different study designs. • Awareness of industry and project standards & ICH guidelines. • Excellent verbal and written communication skills. A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page.
Geoff King at RBW Consulting is recruiting for multiple, permanent Senior & Principal Statisticians to join a leading pharmaceutical company as they look to expand their existing teams in the UK and US. This position is office based in London or Hertfordshire with 1-2 days home work flexibility. Senior & Principal level Statisticians are required for this science-led healthcare company who have an incredibly exciting range of products in the pipeline across multiple therapeutic area's including Respiratory, Infectious Disease, Immuno-Inflammatory and more. As a Statistician you will play an important part in delivering the companies mission in helping people to do more, feel better and live longer. As part of a diverse, global team you will have the opportunity to work in an environment where you realise your full potential and achieve your career goals. *Main duties & responsibilities:* * Providing statistical expertise to support the design and interpretation of clinical programs, regulatory submissions and commercialisation * Analysing internal and external information to inform design decisions and the development of decision criteria * Providing support to the regulatory submissions including specification of overview documents and response to regulatory questions * Identifying opportunities for the application of modelling and simulation to improve study design *Key requirements:* * PhD or MSc in Statistics or Biostatistics combined with relevant experience within the pharmaceutical industry * Advanced knowledge of clinical study designs and common statistical analysis methods * Extensive knowledge of FDA and ICH regulations and industry standards * Good knowledge of statistical programming languages and statistical software (eg. SAS, R, East etc) * Excellent communication skills A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.
Mar 23, 2021
Full time
Geoff King at RBW Consulting is recruiting for multiple, permanent Senior & Principal Statisticians to join a leading pharmaceutical company as they look to expand their existing teams in the UK and US. This position is office based in London or Hertfordshire with 1-2 days home work flexibility. Senior & Principal level Statisticians are required for this science-led healthcare company who have an incredibly exciting range of products in the pipeline across multiple therapeutic area's including Respiratory, Infectious Disease, Immuno-Inflammatory and more. As a Statistician you will play an important part in delivering the companies mission in helping people to do more, feel better and live longer. As part of a diverse, global team you will have the opportunity to work in an environment where you realise your full potential and achieve your career goals. *Main duties & responsibilities:* * Providing statistical expertise to support the design and interpretation of clinical programs, regulatory submissions and commercialisation * Analysing internal and external information to inform design decisions and the development of decision criteria * Providing support to the regulatory submissions including specification of overview documents and response to regulatory questions * Identifying opportunities for the application of modelling and simulation to improve study design *Key requirements:* * PhD or MSc in Statistics or Biostatistics combined with relevant experience within the pharmaceutical industry * Advanced knowledge of clinical study designs and common statistical analysis methods * Extensive knowledge of FDA and ICH regulations and industry standards * Good knowledge of statistical programming languages and statistical software (eg. SAS, R, East etc) * Excellent communication skills A comprehensive job description is available upon request. To find out more about this fantastic opportunity or to discuss other open positions which may be of interest please contact Geoff King on (0) and send your CV through to [](mailto:) or use the apply button on this page. If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential.